Baxter Healthcare Corporation
Baxter Healthcare Corporation sponsors 46 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 34 completed. 12 of these trials are in Phase 3-4 (later-stage) and 9 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Hypertension, with 2 trials.
Trial Pipeline
46 total, page 1 of 1
Gen 2 Battrode Wear Study
NCT07256951
Tympanic Thermometer Study
NCT06556628
Mobile Cardiac Telemetry (MCT) Study
NCT07158333
A Study Comparing Organic Phosphate (Sodium Glycerophosphate Injection) to Numeta G16%E
NCT06842134
A Bioequivalence Study Comparing Organic Phosphate (Sodium Glycerophosphate Injection) to Inorganic Phosphate (Sodium Phosphates Injection, USP)
NCT06842121
PMCF Study for COSEAL® in Gynecologic Surgery
NCT05996809
Timmy3 Module Clinical Accuracy ISO 80601-2-56:2017 + A1 2018
NCT06056011
PMCF Study for ADEPT® in LaparoscopicGynecologic Surgery
NCT05811585
DermaClose DUKE Fasciotomy and Wound Study
NCT05330767
Cefazolin PK Study 3g vs 2g
NCT05309304
Oscillation and Lung Expansion (OLE) Therapy for Treatment of Neuromuscular Disease (NMD) Patients
NCT05366010
Pediatric Study to Evaluate Risk of Developing Essential Fatty Acid Deficiency When Receiving Clinolipid or Standard-of-Care Lipid Emulsion (Part A)
NCT04555044
Starling Registry Study
NCT04648293
Healthy Volunteer Study to Evaluate the Impact of Various Common Interventions on Venous Pressure Signal Captured by PIVA
NCT04324593
Validation of a Sensor for Non-invasive Measurement of Stroke Volume and Cardiac Output
NCT04255108
Bioequivalence Study Assessing Iron Sucrose or Venofer® in Healthy Adult Subjects
NCT04155814
Observational Study Using the CoVa Monitoring System 3
NCT03884582
Validation of a Sensor for Non-Invasive Measurements
NCT03463148
Remotely Monitoring Patients With Chronic Conditions in Their Home
NCT03207802
Efficacy and Safety of FS VH S/D 500 S-apr (Tisseel) as an Adjunct to Sutured Dural Repair in Cranial Surgery
NCT02891070
Effectiveness and Safety of CELSTAT for Hemostasis in Intraoperative Tissue Bleeding
NCT02640235
Pediatric Study to Evaluate Risk of Developing Essential Fatty Acid Deficiency When Receiving Clinolipid or Standard-of-Care Lipid Emulsion
NCT02476994
Necklace-Shaped Sensor for Non-Invasive Remote Monitoring of Vitals
NCT02337790
Monitoring Subjects With Fluid-Management Issues In the Home Environment
NCT02190877
Neck-Worn Monitoring Sensor for - A Study for Monitoring Subjects With Fluid-Management Issues During Dialysis
NCT02140905
Effects of IV Chloride Content on Outcomes
NCT02083198
Dosing Study of Amino Acids in Seriously Ill Patients
NCT01923480
Efficacy and Safety of FLOSEAL for Hemostasis in Total Knee Arthroplasty
NCT01410240
Veritas in Non-Bridging Ventral Hernia Repair
NCT01426477
Intravenous (IV) Solutions for Dehydration in Children With Gastroenteritis
NCT01234883
Retrospective Analysis of Veritas in Breast Reconstruction
NCT01454713
Efficacy and Safety of ARTISS for Flap Adherence in Abdominoplasty
NCT01112735
Study of In-line Pressure Using Various Techniques of Subcutaneous Administration of Fluids Enabled by Human Recombinant Hyaluronidase (INFUSE-AT1A)
NCT01116102
Efficacy and Safety of FS VH S/D 4 S-apr for Flap Adherence in Rhytidectomy
NCT00999141
Bone Graft Materials Observational Registry
NCT00974623
FS VH S/D 500 S-apr in Vascular Surgery
NCT00892957
The Mechanism of Action of the Unite Biomatrix in Diabetic Foot Ulcer
NCT00958711
Study of Techniques of Subcutaneous Administration of Fluids Enabled by Human Recombinant Hyaluronidase
NCT00807885
Efficacy and Safety Study of Fibrin Sealant With 4 IU/mL Thrombin, Vapor Heated, Solvent Detergent Treated (FS VH S/D 4) in Face-Lift Procedures
NCT00708071
Fibrin Sealant for the Sealing of Dura Sutures
NCT00681824
Fibrin Sealant Vascular Surgery Study
NCT00576420
Peri-Strips Dry (PSD) Veritas Collagen Matrix Staple Line Reinforcement for Colorectal Surgery
NCT00559013
Reinforcement of Surgical Staple Lines Using Peri-Strips Dry (PSD) With Veritas Collagen Matrix
NCT00566943
Safety and Efficacy Study of FS 4 IU VH S/D (Fibrin Sealant With 4IU/mL Thrombin, Vapor Heated, Solvent/Detergent Treated) to Adhere Split Thickness Skin Grafts and Improve Wound Healing in Burn Patients
NCT00157131
Safety and Hemostatic Efficacy of Fibrin Sealant Vapor Heated, Solvent/Detergent Treated (FS VH S/D) Compared With Currently Licensed TISSEEL VH Fibrin Sealant in Subjects Undergoing Cardiac Surgery
NCT00161733
Safety and Efficacy Study of Fibrin Sealant (FS 4IU) for Skin Graft Fixation and Wound Healing in Subjects With Burn Wounds
NCT00161759
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 5 |
| Phase 2 | 4 |
| Phase 3 | 5 |
| Phase 4 | 7 |
Therapeutic Areas
What the Pipeline for Baxter Healthcare Corporation Shows
According to the ClinicalTrials.gov registry, Baxter Healthcare Corporation is linked to 46 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 2% of the sponsor's indexed portfolio, and 34 are already marked complete, representing roughly 74% of the total.
The phase mix for Baxter Healthcare Corporation reports 12 late-stage studies (Phase 3 and Phase 4 combined) and 9 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Baxter Healthcare Corporation is Hypertension with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.